Liu Cuiying, Xu Xianghua, Fan Jianling
Jiangsu Key Laboratory of Agricultural Meteorology, College of Applied Meteorology, Nanjing University of Information Science and Technology, Nanjing 210044, China.
Jiangsu Key Laboratory of Agricultural Meteorology, College of Applied Meteorology, Nanjing University of Information Science and Technology, Nanjing 210044, China.
J Environ Sci (China). 2015 Dec;38:87-94. doi: 10.1016/j.jes.2015.05.005. Epub 2015 Jun 26.
The application of electron donor and electron shuttle substances has a vital influence on electron transfer, thus may affect the reductive dechlorination of 1,1,1-trichoro-2,2-bis(p-chlorophenyl)ethane (DDT) in anaerobic reaction systems. To evaluate the roles of citric acid and anthraquinone-2,6-disulfonate (AQDS) in accelerating the reductive dechlorination of DDT in Hydragric Acrisols that contain abundant iron oxide, a batch anaerobic incubation experiment was conducted in a slurry system with four treatments of (1) control, (2) citric acid, (3) AQDS, and (4) citric acid+AQDS. Results showed that DDT residues decreased by 78.93%-92.11% of the initial quantities after 20days of incubation, and 1,1-dichloro-2,2-bis(4-chlorophenyl)-ethane (DDD) was the dominant metabolite. The application of citric acid accelerated DDT dechlorination slightly in the first 8days, while the methanogenesis rate increased quickly, and then the acceleration effect improved after the 8th day while the methanogenesis rate decreased. The amendment by AQDS decreased the Eh value of the reaction system and accelerated microbial reduction of Fe(III) oxides to generate Fe(II), which was an efficient electron donor, thus enhancing the reductive dechlorination rate of DDT. The addition of citric acid+AQDS was most efficient in stimulating DDT dechlorination, but no significant interaction between citric acid and AQDS on DDT dechlorination was observed. The results will be of great significance for developing an efficient in situ remediation strategy for DDT-contaminated sites.
电子供体和电子穿梭体物质的应用对电子转移具有至关重要的影响,进而可能影响厌氧反应体系中1,1,1 - 三氯 - 2,2 - 双(对氯苯基)乙烷(DDT)的还原脱氯过程。为了评估柠檬酸和蒽醌 - 2,6 - 二磺酸盐(AQDS)在加速富铁氧化物的潜育性强淋溶土中DDT还原脱氯方面的作用,在泥浆体系中进行了批次厌氧培养实验,设置了4种处理:(1)对照;(2)柠檬酸;(3)AQDS;(4)柠檬酸 + AQDS。结果表明,培养20天后,DDT残留量降低了初始量的78.93% - 92.11%,1,1 - 二氯 - 2,2 - 双(4 - 氯苯基)乙烷(DDD)是主要代谢产物。柠檬酸的添加在最初8天对DDT脱氯有轻微加速作用,同时甲烷生成速率迅速增加,8天后加速作用增强而甲烷生成速率降低。AQDS的添加降低了反应体系的氧化还原电位(Eh值),加速了微生物将Fe(III)氧化物还原为Fe(II),Fe(II)是一种有效的电子供体,从而提高了DDT的还原脱氯速率。柠檬酸 + AQDS的添加对刺激DDT脱氯最有效,但未观察到柠檬酸和AQDS在DDT脱氯方面有显著的相互作用。这些结果对于开发高效的DDT污染场地原位修复策略具有重要意义。